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rs864622393

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACTGCAG;ACTGCAG) 0 common in clinvar
Make rs864622393(-;-)
Make rs864622393(-;CTGCAGA)
Make rs864622393(CTGCAGA;CTGCAGA)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132603352
GeneRAD50
is asnp
is mentioned by
dbSNPrs864622393
dbSNP (old)rs864622393
ClinGenrs864622393
ebirs864622393
HLIrs864622393
Exacrs864622393
Gnomadrs864622393
Varsomers864622393
Maprs864622393
PheGenIrs864622393
Biobankrs864622393
1000 genomesrs864622393
hgdprs864622393
ensemblrs864622393
gopubmedrs864622393
geneviewrs864622393
scholarrs864622393
googlers864622393
pharmgkbrs864622393
gwascentralrs864622393
openSNPrs864622393
23andMers864622393
23andMe allrs864622393
SNP Nexus

SNPshotrs864622393
SNPdbers864622393
MSV3drs864622393
GWAS Ctlgrs864622393
Max Magnitude0
ClinVar
Risk rs864622393(-;-)
Alt rs864622393(-;-)
Reference Rs864622393(ACTGCAG;ACTGCAG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131939044_131939050delCTGCAGA
CLNSRC
CLNACC RCV000205373.1,